CAS 7236-57-9
:1-(2-deoxy-beta-D-erythro-pentofuranosyl)-5-methyl-4-thioxo-3,4-dihydropyrimidin-2(1H)-one
Description:
1-(2-Deoxy-beta-D-erythro-pentofuranosyl)-5-methyl-4-thioxo-3,4-dihydropyrimidin-2(1H)-one, with the CAS number 7236-57-9, is a nucleoside analog that exhibits structural features characteristic of both nucleosides and pyrimidine derivatives. This compound contains a 2-deoxy-pentofuranosyl moiety, which is a sugar component commonly found in DNA, linked to a pyrimidinone structure that includes a thioxo group, contributing to its potential biological activity. The presence of the methyl group at the 5-position of the pyrimidine ring may influence its pharmacological properties, including its interaction with biological targets such as enzymes or receptors. This compound has garnered interest in medicinal chemistry for its potential antiviral or anticancer properties, as many nucleoside analogs are designed to interfere with nucleic acid synthesis. Its solubility, stability, and reactivity can vary based on environmental conditions, making it a subject of study in drug development and biochemical research.
Formula:C10H14N2O4S
InChI:InChI=1/C10H14N2O4S/c1-5-3-12(10(15)11-9(5)17)8-2-6(14)7(4-13)16-8/h3,6-8,13-14H,2,4H2,1H3,(H,11,15,17)/t6-,7+,8+/m0/s1
Synonyms:- 1-(2-deoxypentofuranosyl)-5-methyl-4-thioxo-3,4-dihydropyrimidin-2(1H)-one
- Thymidine, 4-thio-
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Found 6 products.
4-Thiothymidine
CAS:Formula:C10H14N2O4SPurity:≥ 98.0%Color and Shape:Off-white to yellow powderMolecular weight:258.34-Thiothymidine
CAS:<p>4-Thiothymidine is a Nucleoside Derivative - Thio-nucleoside, 5-Modified pyrimidine nucleoside.</p>Formula:C10H14N2O4SPurity:99.92%Color and Shape:SolidMolecular weight:258.294-Thiothymidine
CAS:<p>4-Thiothymidine is a nucleoside analog that is converted to thymidine by the enzyme thymidine kinase. It has been shown to inhibit the growth of human skin cancer cells by binding to DNA duplexes and inhibiting the synthesis of new DNA strands. 4-Thiothymidine has also been shown to be effective against radiation-induced damage in cultured human cells and inhibits tumor growth in mice bearing a transplantable mouse skin cancer. 4-Thiothymidine can be used as an inhibitor for chemotherapy or radiation therapy for cancer patients. It is active on both site-specific and cell-specific gene targets, with a reactive hydrogen bond that helps stabilize its formation.</p>Formula:C10H14N2O4SPurity:Min. 98 Area-%Color and Shape:Yellow PowderMolecular weight:258.3 g/mol





